MDR training events

We offer a range of training events to familiarise stakeholders from across the industry to all aspects of the new MDR. Our training is targeted for:

  • Product Specialists
  • Regulatory Managers
  • CEOs
  • CFOs
  • Anyone who wants to learn more about the new regulations

Benefit from the clinical knowledge of our specially-trained medical professionals and learn how to integrate their expertise into your MDR compliance strategy.

  1. Online workshop Build a winning MDR compliance strategy

    • Date: 7th July 2020
    • Delegate fee: £350

    This is now fully subscribed. Please see our other available events.

  2. Online workshop Software as a medical device — a guide to MDR compliance

    • Date: 8th July 2020
    • Delegate fee: £350

    This is now fully subscribed. Please see our other available events.

  3. Online workshop Build a winning MDR compliance strategy

    • Understand the MDR in detail and become comfortable working with the MDR as a tool.
    • Eliminate reliance on misleading and inaccurate secondary sources.
    • Apply your understanding of the MDR to build strategies in Risk Management, PMS, PMCF, Vigilance, Gap Analysis and Clinical Evaluation that will drive MDR compliance of your company.
    • Date: 4th August 2020
    • Delegate fee: £350

    More information about the Build a winning MDR compliance strategy online workshop

  4. Online workshop Software as a medical device — a guide to MDR compliance

    • Understand medical device legislation as it applies to software.
    • Learn how to apply the MDR to software as a medical device.
    • Understand how software features will impact product risk classification and requirements for conformity assessment.
    • Build an MDR compliance strategy to ensure regulatory approval of your software product and protect your market position.
    • Date: 5th August 2020
    • Delegate fee: £350

    More information about the Software as a medical device — a guide to MDR compliance online workshop

  5. Live seminar Clinical evidence in the MDR

    • Develop a new level of confidence in applying clinical evidence to your MDR compliance strategy.
    • Understand how to use clinical evidence in MDR Gap Analysis, PMS, PMCF and Clinical Evaluation.
    • Understand aspects of clinical evidence interpretation that you always felt were beyond your grasp and feel confident in handling all types of clinical data.
    • Develop a deep understanding of study power, study types, significance levels and other technical elements that will boost your competence in working with clinical evidence.
    • Date: 9th September 2020
    • Delegate fee: £650 (includes lunch & refreshments)

    More information about the Clinical evidence in the MDR online workshop

  6. Live seminar MDR Compliance for Class I devices

    • Understand the specific requirements for MDR compliance of Class I medical devices.
    • Understand how requirements differ from those under MDD.
    • Learn what to do to prepare your regulatory strategy for full implementation of the MDR.
    • Date: 16th September 2020
    • Delegate fee: £650 (includes lunch & refreshments)

    More information about the MDR Compliance for Class I devices online workshop

  7. Live seminar MDR Compliance for CEOs/CFOs

    • A seminar specifically geared towards senior company decision makers who require an overview of the MDR and what it means for their company.
    • Delivered by a fellow company founder, this seminar focuses on business-critical aspects of MDR compliance that will ensure you maintain regulatory approval of your products after May 2021.
    • Date: 23rd September 2020
    • Delegate fee: £650 (includes lunch & refreshments)

    More information about the MDR Compliance for CEOs/CFOs online workshop

  8. Live seminar Clinical evaluation for Class III devices — do you have what it takes?

    • An in-depth exploration of preparing towards and conducting clinical evaluation of Class III medical devices.
    • Understand the impact of this risk classification on designing and implementing clinical evaluation activities.
    • Date: 30th September 2020
    • Delegate fee: £650 (includes lunch & refreshments)

    More information about the Clinical evaluation for Class III devices — do you have what it takes? online workshop

Stay informed

Subscribe to our newsletter and get free access to our MDR downloads.

You will be subscribed to our email newsletter and be given access to our downloads. You can unsubscribe at any time. Your privacy is important. See how we handle your data.

Any questions?

If you have any questions about our MDR training, please get in touch.

Request callback

Download our free Mastering the MDR White Paper

Download

MDR Services

Our team of medical doctors are specialists at building the clinical evidence portfolio that you need for MDR compliance of your products.

  • Through our bespoke Post-Market Surveillance (PMS) service we will apply clinical knowledge to design, update, implement, and maintain your MDR compliant PMS systems.

    Learn more about our Post-Market Surveillance service

    • Designing your PMS system
    • Vigilance systems
    • Medical complaints
    • Writing PMS plans & PSURs
    • Clinical investigations & product registries
    • Risk management
    • Identify needs for any PACAs / FSCAs
  • Our medical experts will design a robust and adaptable clinical evidence generation system to collect Post-Market Clinical Follow-up (PMCF) data on your medical devices.

    Learn more about our Post-Market Clinical Follow-up service

    • Design your PMCF strategy
    • Build Medical Device Product Registries
    • Ensure complete lifecycle evidence generation
    • Prepare evidence reports for other departments
    • Reduce time waste on administration
  • Our full Clinical Evaluation service involves a 360-degree analysis of your medical devices, writing and reviewing CERs, and designing clinical development plans.

    Learn more about our Clinical Evaluation service

    • Performing 360-degree Clinical Evaluations
    • Write & review CERs
    • Systematic literature appraisals
    • Clinical evidence Gap Analyses
    • Clinical development plans
    • Designing & implementing clinical investigations
  • Our medics will apply powerful clinical techniques to quickly and effectively identify and minimise any gaps in your clinical evidence portfolio.

    Learn more about our Gap Analysis service

    • Identify your product's general SPRs
    • Find gaps in existing evidence portfolio
    • Systematic literature reviews
    • Clinical development plans
    • Impact analysis on Risk Management processes

Do you have any questions about our services or training?

Contact us